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FDAMarch 3, 2026device

Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838085268008848380992580088483811677100884838110571

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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